Canonical Allele Identifier: PA2825611494
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 822635

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119587.1:p.Leu157Phe
CA397836616
NM_001126115.1:c.469C>T